A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156622



Internal ID22087023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169523035..169582642hg38UCSC Ensembl
Outerchr6:169521284..169587869hg38UCSC Ensembl
Innerchr6:169923130..169982738hg19UCSC Ensembl
Outerchr6:169921379..169987965hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3866586
hg1966587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022845
Samples
Known GenesWDR27
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156622
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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